Class Class II

Oxiplex® (DEN240038)

DEN240038 2025-06-17 Direct
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Description

Oxiplex® by Fziomed, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberDEN240038
Clearance Date2025-06-17
Clearance TypeDirect
Product CodeQVL
Regulation Number888.3047

Categories

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